QA Specialist

Only candidates living within a commutable distance to Breda and able to start quickly will be considered.

Our client is looking for a QA Specialist who will play a key role in ensuring GMP compliance across equipment, automation, and information systems. In this role, you will support validation activities, guide operational teams on quality requirements, and act as a subject-matter expert in core QA processes such as change control and quality risk management.

What You’ll Do

• Provide QA support and oversight for validation of equipment, automation, and information systems.
• Review and approve validation documentation, ensuring compliance with Corporate, Site, and Regulatory standards.
• Align on validation strategies together with PD, Maintenance & Engineering, and IS teams, providing clear guidance on design, characterization, and validation activities.
• Review and approve equipment-related changes (e.g., parameter updates, like-for-like assessments).
• Review and approve changes to M&E procedures, including changeover processes and maintenance activities
• Manage device-related responsibilities and ensure alignment with all relevant GMP regulations.
• Represent QA in QRM activities such as pFMEA, QRAES, and computer system compliance.
• Ensure site-level Quality Risk activities align with corporate policies and strategy.
• Review and assess QRM reports.
• Perform final QA review of technical change controls, ensuring stakeholder assessments are complete and accurately documented
• Act as QA Subject Matter Expert, collecting input from multiple QA areas to provide a complete QA assessment for technical changes.